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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1442638생성일: 2026년 10월 27일

Potassium methyl N-cyanodithioimidocarbonate → 3-(4-Amino-2-methylsulfanyl-thiazol-5-yl)-2-cyano-3-oxo-propionic acid tert-butyl ester

https://huagongshe.com/reaction/1442638

반응식

참여 물질

역할이름HCID투입량
반응물Potassium methyl N-cyanodithioimidocarbonateHCID 2733091—
반응물4-Chloro-2-cyano-3-hydroxy-but-2-enoic acid tert-butyl esterHCID 76837579—
용매AcetoneHCID 180—
생성물3-(4-Amino-2-methylsulfanyl-thiazol-5-yl)-2-cyano-3-oxo-propionic acid tert-butyl esterHCID 68540342—

반응 단계

To a stirred solution of 4-chloro-2-cyano-3-hydroxy-but-2-enoic acid tert-butyl ester Compound 1c (51.3 g, 236 mmol) at 0° C. in acetone (750 mL) was added potassium methyl N-cyanodithioimidocarbonate Compound 1e (40.2 g, 236 mmol). After 1 hr the reaction was allowed to warm to RT. The reaction mixture was evaporated down after stirring for 18 hrs. The resulting residue was extracted with ethyl acetate from saturated NaHCO3. The combined organic layers were dried over MgSO4 and the solvent removed under reduced pressure to yield a tan foam, 3-(4-amino-2-methylsulfanyl-thiazol-5-yl)-2-cyano-3-oxo-propionic acid tert-butyl ester Compound 1h, 72.2 g. 1H NMR (CDCl3) δ 4.34 (br s, 2H), 3.14 (br s, 1H), 2.70 (br s, 3H), 1.47 (br s, 9H). MS 314 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07659284B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-8aafb594f24d4c63800e65f8ca8aeeb0
출처 메모uspto-grants-2010_02